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HRID 2386648作成日:2026年10月26日

Iodoethane → 3-butyl-1-ethyl-7-(phenylmethyl)-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/2386648

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Potassium CarbonateHCID 11430—
反応物7-Benzyl-3-butylxanthineHCID 3993866—
溶媒DimethylformamideHCID 6228—
生成物3-butyl-1-ethyl-7-(phenylmethyl)-3,7-dihydro-1H-purine-2,6-dioneHCID 59299554—

反応手順

3-butyl-7-(phenylmethyl)-3,7-dihydro-1H-purine-2,6-dione (0.429 g, 1.24 mmol) and potassium carbonate (0.256 g, 1.85 mmol) were suspended in DMF (8 mL), iodoethane (0.113 mL, 1.42 mmol) was added. The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was evaporated to dryness and the residue was partitioned between water and ethyl acetate. The organic layer was washed with water, followed by brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to yield the title compound; 1H NMR (400 MHz; CDCl3) δ: 0.96 (3H, t), 1.25 (3H, t), 1.36-1.45 (2H, m), 1.72-1.76 (2H, m), 4.05-4.13 (4H, m), 5.50 (2H, s), 7.32-7.40 (5H, m), 7.52 (1H, s); m/z 327 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08268839B2
出典データセットuspto-grants-2012_09
ORD IDord-2e10334914be4a08a70f1a4a74503b87
出典メモuspto-grants-2012_09